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10 sources retrieved Β· Most recent: April 2026 Β· Index updated 14 days ago
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SLC17A9
solute carrier family 17 member 9
Chromosome 20 Β· 20q13.33
NCBI Gene: 63910Ensembl: ENSG00000101194.19HGNC: HGNC:16192UniProt: Q9BYT1
27PubMed Papers
21Diseases
0Drugs
1Pathogenic Variants
FUNCTIONAL ROLE
Transporter
CLINICAL
OMIM Disease Gene
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
ADP transportguanine nucleotide transmembrane transportATP exportguanine nucleotide transmembrane transporter activitydisseminated superficial actinic porokeratosisjaw diseasenonpapillary renal cell carcinomahepatocellular carcinoma
✦AI Summary

SLC17A9 (solute carrier family 17 member 9) is a voltage-gated ATP nucleotide uniporter that transports ATP, ADP, and GTP across vesicular membranes using the membrane potential as the driving force 1. Primarily localized to lysosomes and secretory vesicles, SLC17A9 regulates ATP accumulation in lysosomes and controls ATP-dependent lysosomal proteins, while indirectly regulating ATP exocytosis in astrocytes, adrenal chr20 granules, and synaptic vesicles 123. SLC17A9 deficiency impairs lysosomal ATP content and compromises cell viability 3. Beyond normal physiology, SLC17A9 has emerged as a significant oncogenic modulator. Elevated SLC17A9 expression correlates with poor prognosis in multiple cancers: colorectal, gastric, and lung cancer, where it serves as an independent prognostic predictor 456. In clear cell renal cell carcinoma, SLC17A9 promotes cell growth and migration through KCNH1 regulation 7. In hepatocellular carcinoma, the HHEX-mediated ABI2/SLC17A9 axis maintains cancer stem cell properties 8. Additionally, SLC17A9 genetic polymorphisms are associated with phantom tooth pain susceptibility, suggesting roles in neuropathic pain pathways 9. Cardiac studies demonstrate SLC17A9-dependent ATP release from sympathetic neurons regulates NLRP3 inflammasome activation and pressure overload-induced cardiac hypertrophy 10.

Sources cited
1
SLC17A9 (solute carrier family 17 member 9) is a voltage-gated ATP nucleotide uniporter that transports ATP, ADP, and GTP across vesicular membranes using the membrane potential as the driving force .
PMID: 18375752
2
Primarily localized to lysosomes and secretory vesicles, SLC17A9 regulates ATP accumulation in lysosomes and controls ATP-dependent lysosomal proteins, while indirectly regulating ATP exocytosis in astrocytes, adrenal chr20 granules, and synaptic vesicles , , .
PMID: 24962569
3
In clear cell renal cell carcinoma, SLC17A9 promotes cell growth and migration through KCNH1 regulation .
PMID: 40302348
4
In hepatocellular carcinoma, the HHEX-mediated ABI2/SLC17A9 axis maintains cancer stem cell properties .
PMID: 38844969
5
Additionally, SLC17A9 genetic polymorphisms are associated with phantom tooth pain susceptibility, suggesting roles in neuropathic pain pathways .
PMID: 35266813
6
Cardiac studies demonstrate SLC17A9-dependent ATP release from sympathetic neurons regulates NLRP3 inflammasome activation and pressure overload-induced cardiac hypertrophy .
PMID: 36440584
Disease Associationsβ“˜21
disseminated superficial actinic porokeratosisOpen Targets
0.64Moderate
jaw diseaseOpen Targets
0.26Weak
nonpapillary renal cell carcinomaOpen Targets
0.08Suggestive
hepatocellular carcinomaOpen Targets
0.08Suggestive
MODYOpen Targets
0.08Suggestive
posterior cortical atrophyOpen Targets
0.07Suggestive
Combined pituitary hormone deficiencies, genetic formsOpen Targets
0.07Suggestive
type 1 diabetes mellitusOpen Targets
0.07Suggestive
neoplasmOpen Targets
0.07Suggestive
hyperinsulinism due to glucokinase deficiencyOpen Targets
0.06Suggestive
hyperinsulinism due to INSR deficiencyOpen Targets
0.06Suggestive
Barrett's esophagusOpen Targets
0.06Suggestive
diabetes mellitusOpen Targets
0.06Suggestive
exercise-induced hyperinsulinismOpen Targets
0.05Suggestive
hypoinsulinemic hypoglycemia and body hemihypertrophyOpen Targets
0.05Suggestive
maturity-onset diabetes of the young type 4Open Targets
0.05Suggestive
hypopituitarismOpen Targets
0.05Suggestive
hyperinsulinism-hyperammonemia syndromeOpen Targets
0.05Suggestive
Adrenocorticotropic hormone deficiencyOpen Targets
0.05Suggestive
short stature due to partial GHR deficiencyOpen Targets
0.05Suggestive
Porokeratosis 8, disseminated superficial actinic typeUniProt
Pathogenic Variants1
NM_022082.4(SLC17A9):c.932G>A (p.Arg311Gln)Pathogenic
Porokeratosis 8, disseminated superficial actinic type
β˜†β˜†β˜†β˜†2014β†’ Residue 311
View on ClinVar β†—
Related Genes
SLC25A25Shared pathway67%SLC35B1Shared pathway67%SLC25A42Shared pathway50%SLC25A41Shared pathway40%SLC25A43Shared pathway33%SLC25A17Shared pathway33%
Tissue Expression6 tissues
Liver
100%
Bone Marrow
9%
Lung
7%
Ovary
2%
Heart
1%
Brain
0%
Gene Interaction Network
Click a node to explore
SLC17A9SLC25A25SLC35B1SLC25A42SLC25A41SLC25A43SLC25A17
PROTEIN STRUCTURE
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AlphaFoldAI-predicted Β· UniProt Q9BYT1
View on AlphaFold β†—
Constraintβ“˜
LOEUFβ“˜
1.15LoF Tolerant
pLIβ“˜
0.00Tolerant
Observed/Expected LoF0.91 [0.72–1.15]
RankingsWhere SLC17A9 stands among ~20K protein-coding genes
  • #12,671of 20,598
    Most Researched27
  • #5,292of 5,498
    Most Pathogenic Variants1
  • #11,918of 17,882
    Most Constrained (LOEUF)1.15
Genes detectedSLC17A9
Sources retrieved10 papers
Response timeβ€”
πŸ“„ Sources
10β–Ό
1
NLRP3 Inflammasome Activation Through Heart-Brain Interaction Initiates Cardiac Inflammation and Hypertrophy During Pressure Overload.
PMID: 36440584
Circulation Β· 2023
1.00
2
The HHEX-ABI2/SLC17A9 axis induces cancer stem cell-like properties and tumorigenesis in HCC.
PMID: 38844969
J Transl Med Β· 2024
0.90
3
Co-Highly Expressed
PMID: 40302348
Front Biosci (Landmark Ed) Β· 2025
0.80
4
Single-nucleotide polymorphisms of the SLC17A9 and P2RY12 genes are significantly associated with phantom tooth pain.
PMID: 35266813
Mol Pain Β· 2022
0.70
5
[Strategies for Transporter-targeted Drug Discovery].
PMID: 33790115
Yakugaku Zasshi Β· 2021
0.60